山田俊一 | Faculty Of Pharmaceutical Sciences University Of Tokyo

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山田俊一
Faculty Of Pharmaceutical Sciences University Of Tokyo
山田俊一
Faculty of Pharmaceutical Sciences, University of Tokyo
塩入孝之
Faculty Of Pharmaceutical Sciences Nagoya City University
寺島孜郎
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)sagami Chemical Research Cen
塩入孝之
Faculty of Pharmaceutical Sciences, Nagoya City University
寺島孜郎
(財)相模中央化学研究所
古賀憲司
Faculty of Pharmaceutical Sciences, University of Tokyo
Koga Kenjiro
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Hokuriku University
寺島孜郎
Faculty of Pharmaceutical Sciences, University of Tokyo
山田俊一
東京大学
阿知波一雄
Faculty of Pharmaceutical Sciences, University of Tokyo
広井邦雄
Faculty Of Pharmaceutical Sciences University Of Tokyo
菊川靖雄
Faculty of Pharmaceutical Sciences, Josai University
菊川靖雄
Faculty Of Pharmaceutical Sciences Josai University
大谷元治
Tokyo Research Laboratories Kowa Company Ltd.
柴崎正勝
東大院薬
柴崎正勝
Faculty Of Pharmaceutical Sciences Teikyo University:(present Address)faculty Of Pharmacertical Scie
高村則夫
Organic Chemistry Research Laboratory, Tanabe Seiyaku Co., Ltd.,
松尾寿之
Faculty Of Pharmaceutical Sciences University Of Tokyo
国枝武久
Faculty of Pharmaceutical Sciences, University of Tokyo
藤井澄三
Faculty Of Pharmaceutical Sciences Kanazawa University
竹内義雄
Faculty Of Pharmaceutical Sciences University Of Tokyo
柴崎正勝
Faculty Of Pharmaceutical Sciences Hokkaido University
高村則夫
Organic Chemistry Research Laboratory Tanabe Seiyaku Co. Ltd.
大谷元治
Faculty of Pharmaceutical Sciences, University of Tokyo
国枝武久
Faculty Of Pharmaceutical Sciences Kumamoto University
石川清康
Faculty Of Pharmaceutical Sciences University Of Tokyo
水野初彦
Faculty of Pharmaceutical Sciences, Osaka University
斎藤勲
Faculty Of Pharmaceutical Sciences University Of Tokyo
池上四郎
Faculty of Pharmaceutical Sciences, Teikyo University
水野初彦
Faculty Of Pharmaceutical Sciences University Of Tokyo
高村則夫
Faculty of Pharmaceutical Sciences, University of Tokyo
畑俊輔
Research Laboratory, Mitsubishi Yuka Pharmaceutical Co., Ltd.
小栗東明
Faculty of Pharmaceutical Sciences, University of Tokyo
関谷哲雄
Pharmaceuticals Laboratory, Research Center, Mitsubishi Kasei Corporation
畑俊輔
Research Laboratory Mitsubishi Yuka Pharmaceutical Co. Ltd.
池上四郎
Faculty Of Pharmaceutical Sciences Teikyo University
関谷哲雄
Pharmaceuticals Laboratory Research Center Mitsubishi Kasei Corporation
小栗東明
Faculty Of Pharmaceutical Sciences University Of Tokyo
アブドールーモハッセンエム.イー.オマール
Faculty of Pharmaceutical Sciences, University of Tokyo
山田俊一
東京大学薬学部
北本六良
Faculty of Pharmaceutical Sciences, University of Tokyo
関谷哲雄
Research Laboratory, Mitsubishi Yuka Pharmaceutical Co., Ltd.
富岡清
Faculty of Pharmaceutical Sciences, University of Tokyo
曽根孝範
Faculty of Pharmaceutical Sciences, University of Tokyo
倉本正志
Faculty of Pharmaceutical Sciences, University of Tokyo
我妻光吉
Faculty of Pharmaceutical Sciences, University of Tokyo
曽根孝範
Life-science Institute, Asahi Chemical Industry Co., Ltd.
曽根孝範
Life-science Institute Asahi Chemical Industry Co. Ltd.
我妻光吉
Faculty Of Pharmaceutical Sciences University Of Tokyo
石墨紀久夫
Sumitomo Pharmaceuticals Research Center
アブドールーモハッセンエム.イー.オマール
Faculty Of Pharmaceutical Sciences University Of Tokyo
呉欽敬
Faculty Of Pharmaceutical Sciences University Of Tokyo
石墨紀久夫
Faculty of Pharmaceutical Sciences, University of Tokyo
倉本正志
Faculty Of Pharmaceutical Sciences University Of Tokyo
北本六良
Faculty Of Pharmaceutical Sciences University Of Tokyo
日野亨
Faculty of Pharmaceutical Sciences, Chiba University
浜田康正
Faculty of Pharmaceutical Sciences, Nagoya City University
佐藤忠夫
Faculty Of Pharmaceutical Sciences Chiba University
関英男
Faculty of Pharmaceutical Sciences, University of Tokyo
橋本俊一
Faculty Of Pharmaceutical Sciences University Of Tokyo
日野亨
The Chemical Analysis Center Chiba University:faculty Of Pharmaceutical Sciences Chiba University
長沢一男
東京大学薬学部
広井邦雄
東京大学薬学部
塩入孝之
名古屋市大・薬
曽仲奇
Faculty Of Pharmaceutical Sciences University Of Tokyo
伊古田暢夫
Faculty of Pharmaceutical Sciences, University of Tokyo
岡村久也
Kyorin Chemical Laboratory, Kyorin Pharmuceutical Co., Ltd.
村戸和夫
Faculty of Pharmaceutical Sciences, University of Tokyo
二宮邦博
Faculty of Pharmaceutical Sciences, University of Tokyo
関英男
Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
谷口誠朗
東大薬
伊古田暢夫
National Institute Of Radiological Sciences
長沢一男
北海道薬大
谷口誠朗
Faculty of Pharmaceutical Sciences, University of Tokyo
橋本俊一
Faculty Of Pharmaceutical Sciences Hokkaido University
岡村久也
Kyorin Chemical Laboratory Kyorin Pharmuceutical Co. Ltd.
村戸和夫
Faculty Of Pharmaceutical Sciences University Of Tokyo
二宮邦博
Faculty Of Pharmaceutical Sciences University Of Tokyo
李功固
Faculty of Pharmaceutical Sciences, University of Tokyo
Abdul-mohsen M.e.
(present Address)faculty Of Pharmacy Alexandria University
李功固
Faculty Of Pharmaceutical Sciences University Of Tokyo
大石篤郎
Organic Chemistry Research Laboratory, Tanabe Seiyaku Co., Ltd.
近田美紀彦
Organic Chemistry Research Laboratory, Tanabe Seiyaku Co., Ltd.
大石篤郎
Organic Chemistry Research Laboratory Tanabe Seiyaku Co. Ltd.
村上泰興
Faculty of Pharmaceutical Sciences, University of Tokyo
橘真郎
Faculty of Pharmaceutical Sciences, University of Tokyo
大木貞雄
Tokyo College of Pharmacy
松尾市郎
Medical School, Self Defence Force
村上泰興
東邦大学薬学部
小川清美
Faculty of Pharmaceutical Sciences, University of Tokyo
長島弘
Gifu Pharmaceutical University
高橋久紀
東京大学薬学部
曾根孝範
Faculty of Pharmaceutical Sciences, University of Tokyo
五味保男
東京大学薬学部
五味保男
Faculty Of Pharmaceutical Sciences Kanazawa University
小林通洋
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)research Laboratory Kissei P
板谷泰助
Faculty of Pharmaceutical Sciences, Kanazawa University
高木敬次郎
Faculty of Pharmaceutical Sciences, University of Tokyo
北川富造
Faculty of Pharmaceutical Sciences, University of Tokyo
石川清康
Faculty of Pharmaceutical Sciences, University of Tokyo
溝口富茂
Organic Chemistry Research Laboratory Tanabe Seiyaku Co. Ltd.
高木敬次郎
Department Of Pharmacotherapeutics Faculty Of Pharmaceutical Sciences Science University Of Tokyo
原健
Teijin Institute for Bio-medical Research
大橋尚仁
東大薬
松尾市郎
Junsei Pure Chemicals Co. Ltd.
荘祚敏
Institute of Applied Chemistry, National Chiao-Tung University
今田悟史
Research Laboratory, Mitsubishi Yuka Pharmaceutical Co., Ltd.
鈴木喜久次
Daiichi Pure Chemicals Co., Ltd. Funabori Research Laboratory
平沼英敏
Research Laboratory, Mitsubishi Yuka Pharmaceutical Co., Ltd.
内出政之
Research Laboratory, Mitsubishi Yuka Pharmaceutical Co., Ltd.
米島伸泰
Faculty of Pharmaceutical Sciences, University of Tokyo
清水公博
Faculty of Pharmaceutical Sciences, University of Tokyo
奈良宗彦
興和(株)東研
河合伸高
Faculty of Pharmaceutical Sciences, University of Tokyo
大橋尚仁
Faculty of Pharmaceutical Sciences, University of Tokyo
橘真郎
エーザイ
橘真郎
Research Laboratories Eisai Co. Ltd.
亀尾一弥
Faculty of Pharmaceutical Sciences, University of Tokyo
明田耕一
Faculty of Pharmaceutical Sciences, University of Tokyo
高島克己
Faculty of Pharmaceutical Sciences, University of Tokyo
金山敏司
Pharmaceuticals Laboratory, Resaerch Center, Mitsubishi Kasei Corporation
鍛冶健司
Gifu Pharmaceutical University
北川富造
東大薬
横山祐作
Faculty of Pharmaceutical Sciences, University of Tokyo
小沢健志
Faculty of Pharmaceutical Sciences, University of Tokyo
近田美紀彦
The Organic Chemistry Research Laboratory of Tanabe Seiyaku Co. Ltd.
秋元浩
Faculty of Pharmaceutical Sciences, University of Tokyo
岡村久也
Faculty of Pharmaceutical Sciences, University of Tokyo
勇伊実
Faculty of Pharmaceutical Sciences, University of Tokyo
川瀬雅子
Faculty of Pharmaceutical Sciences, University of Tokyo
国久昌弘
Faculty of Pharmaceutical Sciences, University of Tokyo
大谷元治
興和(株)東京研究所
松下誠之
Faculty of Pharmaceutical Sciences, University of Tokyo
鍛治健司
岐阜薬科大学
米島伸泰
Pharmaceutical Research Laboratory Kirin Brewery Co. Ltd.
曾根孝範
Faculty Of Pharmaceutical Sciences University Of Tokyo
明田耕一
Faculty Of Pharmaceutical Sciences University Of Tokyo
小沢健志
Faculty Of Pharmaceutical Sciences University Of Tokyo
亀尾一弥
Research Center Taisho Pharmaceutical Co. Ltd.
松枝礼
New Lead Research Laboratories Sankyo Co. Ltd.
河合伸高
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)central Research Laboratorie
秋元浩
Faculty Of Pharmaceutical Sciences University Of Tokyo
国久昌弘
Faculty Of Pharmaceutical Sciences University Of Tokyo
小川清美
Faculty Of Pharmaceutical Sciences University Of Tokyo
関秀雄
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)fujisawa Pharmaceutical Co.
渡辺寛敏
Faculty of Pharmaceutical Sciences, University of Tokyo
清水公博
Faculty Of Pharmaceutical Sciences University Of Tokyo
原健
Faculty of Pharmaceutical Sciences, University of Tokyo
松枝礼
Faculty of Pharmaceutical Sciences, University of Tokyo
田草川敏朗
Faculty Of Pharmaceutical Sciences University Of Tokyo
近田美紀彦
Organic Chemistry Research Laboratory Tanabe Seiyaku Co. Ltd.
金山敏司
Pharmaceuticals Laboratory Resaerch Center Mitsubishi Kasei Corporation
山本芳光
Faculty Of Pharmaceutical Sciences University Of Tokyo
横山祐作
Faculty Of Pharmaceutical Sciences University Of Tokyo
川瀬雅子
Faculty Of Pharmaceutical Sciences University Of Tokyo
高島克己
Faculty Of Pharmaceutical Sciences University Of Tokyo
勇伊実
Faculty Of Pharmaceutical Sciences University Of Tokyo
荘祚敏
Institute Of Applied Chemistry National Chiao-tung University
内出政之
Research Laboratory Mitsubishi Yuka Pharmaceutical Co. Ltd.
今田悟史
Research Laboratory Mitsubishi Yuka Pharmaceutical Co. Ltd.
荘祚敏
Faculty of Pharmaceutical Sciences, University of Tokyo
RISHI SUSHMA
Faculty of Pharmaceutical Sciences, University of Tokyo
Rishi Sushma
Faculty Of Pharmaceutical Sciences University Of Tokyo
渡辺寛敏
Faculty Of Pharmaceutical Sciences University Of Tokyo
松下誠之
Faculty Of Pharmaceutical Sciences University Of Tokyo
奈良宗彦
Faculty of Pharmaceutical Sciences, University of Tokyo
鈴木喜久次
Daiichi Pure Chemicals Co. Ltd. Funabori Research Laboratory
溝口富茂
Organic Chemistry Research Laboratory, Tanabe Seiyaku Co., Ltd.
楊正勝
Faculty of Pharmaceutical Sciences, University of Tokyo

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著作論文

Amino Acids and Peptides. XXIII. An Asymmetric Synthesis of (R)-(-)-Laudanosine from L-3-(3,4-Dihydroxyphenyl) alanine
Stereochemical Studies. XIII. Determination of the Absolute Configuration of Mercaptosuccinic Acid by Chemical Correlation with Glyceraldehyde
Chemistry of Amino Acids. IV. Decarboxylation of 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid and Its Derivatives
Studies on Opically Active Amino Acids. VII. Stereoselective Synthesis of l-Norephedrine Hydrochloride from D-Phenylalanine
Studies on Optically Active Amino Acids. V. Synthesis of Optically Active α-Aminoalcohols by the Reduction of α-Amino Acid Esters with Sodium Borohydride
Studies on Optically Active Amino Acids. IV. A New Synthetic Approach to Chloramphenicol Base from L-Phenylalanine.
Studies on Thioamides. I. Synthesis of N-(2-Arylethyl)-thioamides and their Infrared Absorption Spectra.
The Reductive Cyclization of 1-Methyl-3-aminoalkyloxindoles with Lithium aluminum Hydride.
Stereochemical Studies. XXXVIII. Asymmetric Synthesis of the Key Compounds for the Synthesis of optically Active Diterpenes. Asymmetric Synthesis of optically Active 1,2,3,4,5,6,7,8,8a-Octahydro-8a-methyl-3,8-naphthalenedione Derivatives with L-Proline De
立体化学の研究(第33報)L-Proline誘導体を用いたEnamineの不斉誘起反応による不斉合成(-)-Bisdehydroestrone Methyl Etherの不斉合成
立体化学の研究(第32報)L-Proline誘導体を用いたEnamineの不斉誘起反応による不斉合成, ステロイドならびにテルペン合成中間体の不斉合成
Stereochemical Studies. XXIX. Asymmetric Synthesis of 2-Alkylcyclohexanones via optically Active Lithioenamines
Stereochemical Studies. XXVIII. Some Aspects of the Asymmetric Synthesis of (R)-(+)-4-Methyl-4-phenyl-2-cyclohexenone via an Enamine
Stereochemical Studies.XX.Asymmetric Synthesis of α-Bromoketones
Stereochemical Studies.XIX. Asymmetric Synthesis of 2-Alkyl-4-substituted Cyclohexanones with Enamine Alkylation
Stereochemical Studies. IX. Asymmetric Synthesis of 2-Alkylcyclo-hexanones with Enamine Alkylation
Chemistry of Amino Acids. V. Studies on α-Alkyl-α-amino Acids. IX. Mild Hydrolytic Ring Cleavage of Hydantoin Derivatives
Studies on Optical Rotatory Dispersion and Circular Dichroism. II. Circular Dichroism of α-Hydroxy-and α-Amino-α-phenyl Ketones
Stereochemical Studies. VII. Thermal Rearrangement of α-Hydroxyimines to α-Aminoketones using optically Active Open Chain Compounds
Studies on optically Active Amino Acids. XVIII. Studies on α-Methyl-α-amino Acids. XIV. Several Optical Properties of α-Methyl-α-amino Acids
Studies on Optically Active Amino Acids. XIV. Studies on α-Alkyl-α-amino acids. VII. Determination of Absolute Configuration of Optically Active α-Methylphenylglycine Configuration of Optically Active α-Methylphenylglycine and 1-Methyl-1-phenylpropylamine
Pyrimidine Derivatives. V. Structure-Activity Studies of Antihypertensive Quinazoline Derivatives Using the Adaptive Least-Squares Method
Pyrimidine Derivatives. VII. Structure-Activity Relationship of Hypoglycemic 4-Amino-2-(1-piperazinyl) pyrimidines investigated by the Adaptive Least-Squares Method
Pyrimidine Derivatives. VI. Synthesis of 2-(1-Piperazinyl)-5,6-polymethylenepyrimidine Derivatives and Determination of Their Hypoglycemic Activity
Stereochemical Studies. LIX. Asymmetric Transamination from (S)-α-Amino Acids. Synthesis of optically Active Amines by Chemical Transamination of (S)-α-Amino Acid Esters to Ketones
SYNTHESIS OF L-TRYPTOPHAN FROM L-GLUTAMIC ACID
Pyrimidine Derivatives. II. New Synthesis and Reactions of 4-Amino-2-methylthiopyrimidine Derivatives
Amino Acids and Peptides. XXX. Phosphorus in Organic Synthesis. XVII. Application of Diphenyl Phosphorazidate (DPPA) and Diethyl Phosphorocyanidate (DEPC) to Solid-phase Peptide Synthesis
Stereoselective Reactions. II. Asymmetric Synthesis of β-Substituted Aldehydes by Michael Reaction using Chiral α, β-Unsaturated Aldimines
Stereoselective Reactions. I. A highly Efficient Asymmetric Synthesis of β-Substituted Aldehydes via 1,4-Addition of Grignard Reagents to optically Active α, β-Unsaturated Aldimines
Stereochemical Studies. LIV. A Biogenetic-type Asymmetric Synthesis of optically Active Galanthamine from L-Tyrosine
Stereochemical Studies. LIII. An Asymmetric Synthesis of (3S 15S 20R)-Yohimbone from L-Tryptophan by 1,3-Transfer of Asymmetry
Synthesis of Formamidines from Carbodiimides with Sodium Borohydride in Isopropanol
Amino Acids and Peptides. XXIX. A New Efficient Asymmetric Synthesis of α-Amino Acid Derivatives with Recycle of a Chiral Reagent-Asymmetric Alkylation of a Chiral Schiff Base from Glycine
Stereochemical Studies. XXIII. Stereochemistry of the Thermal Isocyanide-Cyanide Rearrangement
Stereochemical Studies. XLVII. Asymmetric Reduction of 2-Alkyl-1,3,4-cyclopentanetriones with Lithium Aluminum Hydride decomposed by optically Active β-Aminoalcohols. Syntheses of optically Active Allethrolone and Prostaglandin E_1
Stereochemical Studies. XLV. A Novel Regiospecific Ring Opening of optically Active 2-Substituted-1-tosylaziridines
Stereochemical Studies. XLVI. Studies on the Synthesis of 4-Acetoxy-cyclopentane-1,3-dione Derivatives
Stereochemical Studies. XLIV. Exploitation of the New Synthetic Scheme for Chiral Additives Usable in Asymmetric Syntheses. Novel Syntheses of optically Active γ-Amino Acids and Pyrrolidines from L-α-Amino Acids
Stereochemical Studies. XLIII. Novel Reactivity of Organometallic Reagents to 5,5-Ethylenedioxy-2-methyl-2-phenylcyclohexanone
Stereochemical Studies. XLII. Asymmetric Synthesis of naturally Occurring Podocarpic Acid
Stereochemical Studies. XLI. Asymmetric Synthesis of optically Active 4a-Methyl-4,4a, 9,10-tetrahydro-2 (3H)-phenanthrone Derivatives, Key Intermediates for Total Syntheses of optically Active Diterpenes and Steroids
Stereochemical Studies. XL. A Biomimetic Conversion of L-Lysine into optically Active 2-Substituted Piperidines. Syntheses of D- and L-Pipecolic Acid, and (S) (+)-Coniine from L-Lysine
Stereochemical Studies. XXXIX. A Novel Method for the Preparation of Optically Active Aldehydes. Syntheses of Optically Active (R) (+)-α-Cyclocitral, (S) (+)-Dehydrovomifoliol, and (S) (+)-Abscisic Acid
Stereochemical Studies. XXXV. A Biogenetic-type Asymmetric Cyclization. Syntheses of optically Active α-Cyclocitral and trans-α-Damascone
Stereochemical Studies. XXXIV. A Novel Biogenetic-type Cyclization of Citral to α-Cyclocitral via an Enamine
Stereochemical Studies. XXII. Thermal Rearrangement of S(-)-1-Phenylethyl Isocyanide
The Chemistry of Diborane and Sodium Borohydride. XI. The Reaction of Isoquinoline Reissert Compounds with Sodium Borohydride
Chemistry of Diborane and Sodium Borohydride. X. The Reduction of 2-or 4-Substituted Pyridines and Quinolines, and 1-or 3-Substituted Isoquinolines with Sodium Borohydride
Chemistry of Diborane and Sodium Borohydride. IX. The Reduction of 3-Substituted Pyridines and Quinolines, and 4-Substituted Isoquinolines with Sodium Borohydride
Chemistry of Diborane and Sodium Borohydride. VII. Reduction of α-Amino Acid Amides with Sodium Borohydride
Amino Acids and Peptides. VIII. Phosphorus in Organic Synthesis. III. Synthesis of Some Peptides containing Various Kinds of α-Amino Acids using the Adducts of Phosphorus Compounds and Tetrahalomethanes
Amino Acids and Peptides. VII. Phosphorus in Organic Synthesis. II. A New Method for the Synthesis of Peptides using the Adducts of Phosphorus Compounds and Tetrahalomethanes
Phosphorus in Organic Synthesis. I. A New Method for the Preparation of Amides, Carbamates, Esters, and Carbonates by the Reaction of Alkylidenephosphoranes with Nitrosonium Ion
Amino Acids and Peptides. II. A One-Step Synthesis of Atropine and Other Related Alkaloids from dl-Phenylalanine 3α-Tropanyl Ester
Amino Acids and Peptides. I. Novel Peptide Bond Formation Catalyzed by Metal Ions. I. Formation of Glycine Peptide Esters
Phosphorus in Organic Synthesis. XVI. Diphenyl Phosphorazidate (DPPA) and Diethyl Phosphorocyanidate (DEPC). Two New Reagents for the Preparation of Thiol Esters from Carboxylic Acids and Thiols
Amino Acids and Peptides. XXVIII. A New Synthesis of α-Amino Acid Derivatives by Alkylation of Schiff Bases derived from Glycine and Alanine
Amino Acids and Peptides. XXVII. A Novel Reductive Cleavage of N-C-N Bonds with Sodium Borohydride
Amino Acids and Peptides. XXIV. Phosphorus in Organic Synthesis. XIII. Application of Diphenyl Phosphorazidate (DPPA) to the Synthesis of the Protected N-Terminal Hexapeptide of Secretin
Phosphorus in Organic Synthesis. XII. Amino Acids and Peptides. XXII. Reaction of Penicillin Sulfoxides with Diethyl Phosphorocyanidate (DEPC)
Phosphorus in Organic Synthesis. X. tert-Butyl Carbamate. An Efficient Additive in a Modified Curtius Reaction by Diphenyl Phosphorazidate (DPPA)
Amino Acids and Peptides. XVIII. A Biogenetic-type, Asymmetric Synthesis of (S)-Reticuline from L-3-(3,4-Dihydroxyphenyl)-alanine by 1,3-Transfer of Asymmetry
Amino Acids and Peptides. XVII. A Biogenetic-type, Asymmetric Synthesis of (S)-Laudanosine from L-3-(3,4-Dihydroxyphenyl) alanine by 1,3-Transfer of Asymmetry
Amino Acids and Peptides. XVI. : A New Synthesis of α-Phenylglycine and Its Derivatives
Amino Acids and Peptides. XV. : A New Synthesis of α-Amino Acids by Amination of α-Metalated Carboxylic Acids
Amino Acids and Peptides. XIII. A New Approach to the Biogenetictype, Asymmetric Synthesis of Indole and Isoquinoline Alkaloids by 1,3-Transfer of Asymmetry
Phosphorus in Organic Synthesis. IX. On the Mechanism of Esterification of Malonic Acid Half Esters by Diphenyl Phosphorazidate
Amino Acids and Peptides. XII. Phosphorus in Organic Synthesis. VIII. Reaction of Malonic Acid Half Esters with Diphenyl Phosphorazidate
Amino Acids and Peptides. XI. Phosphorus in Organic Synthesis. VI. Application of Diphenyl Phosphorazidate to the Synthesis of Peptides containing Various Functions
Amino Acids and Peptides. X. Phosphorus in Organic Synthesis. V. On the Mechanism for the Peptide Synthesis by Diphenyl Phosphorazidate
Amino Acids and Peptides. IX. Phosphorus in Organic Synthesis. IV. Diphenyl Phosphorazidate. A New Convenient Reagent for the Peptide Synthesis
Stereochemical Studies. XVII. Nitrous Acid Deaminations of (R)-α-Methylphenylalanine and Its Methyl Ester in Acetic Acid
Stereochemical Studies. XXVII. Total Synthesis of (+)-Mesembrine with Asymmetric Synthesis using Proline Derivative
Stereochemical Studies. XXVI. Asymmetric Synthesis using Proline Derivatives of optically Active Various 4,4-Disubstituted 2-Cyclohexenones with Enamine Alkylation
Stereochemical Studies. XXV. The Absolute Configuration and Optical Purity of (+)-4-Methyl-4-phenyl-2-cyclohexenone
Stereochemical Studies. XXIV. Asymmetric Synthesis of optically Active (+)-4-Methyl-4-phenyl-2-cyclohexenone with Enamine Alkylation using Proline Derivatives
18 不斉合成による(+)-Mesembrineの合成
Preparation of Tyrosol and 4-Methoxyphenethyl Alcohol.
Amino Acids and Peptides. XX. Reduction of α-Substituted α-Diazo Esters. Convenient Synthesis of α-Hydrazinocarboxylic Acids and Their Derivatives from α-Amino Acids
Stereochemical Studies. XXXVI. Stereoselective Syntheses of trans- and cis-Cinnamic Acid Esters from the Phenylalanine Derivatives
Chemistry of Amino Acids. VI. Studies on α-Alkyl-α-amino Acids. X. Unusual Alkyl Migration in the Hofmann Degradation of 5-(2-Dialkylaminoethyl)-5-methylhydantoin Quarternary Ammonium Hydroxide Anhydronium Base
Studies on Optically Active Amino Acids. XV. Studies on α-Alkyl-α-amino Acids. VIII. Absolute Configuration of Optically Active α-Methylserine and 2-Amino-2-methyl-3-butenoic Acid.
Stereochemical Studies. XXI. Studies on α-Alkyl-α-amino Acids. XV. Application of Thermal Isocyanide-Cyanide Rearrangement to R-S Conversion of α-Methylphenylalanine
Chemistry of Diborane and Sodium Borohydride. VI. The Reaction of Amides with Sodium Borohydride
Chemistry of Sodium Borohydride and Diborane. II. Reduction of Schiff Bases with Diborane in Tetrahydrofuran
Chemistry of Sodium Borohydride and Diborane.I. Some New-type of Amine Boranes
Reduction of Acid Amides to Amines with Sodium Borohydride
Chemistry of Sodium Borohydride and Diborane. V. Reduction of Nitrobenzenes with Sodium Borohydride in Pyridine
Amino Acids and Peptides. VI. Novel Peptide Bond Formation catalyzed by Metal Ions. IV. Formation of optically Active Amino Acid Amides and Peptide Amides
Stereochemical Studies. VI. Steric Course of Intramolecular Alkylations using optically Active Amine Derivatives
Studies on Indole Series.I.Studies on the Synthesis of Optically Active Indole Derivatives
Studies on Optical Rotatory Dispersion and Circular Dichroism.I.Absolute Configuration of Cyclic α-Amino-ketones and Octant Rule
Studies on Optically Active Amino Acids.XIII.Racemization of N-Benzoylanilides of Optically Active Proline and Pipecolic Acid
Studies on Optically Active Amino Acids. XII.Synthesis, Resolution and Racemization of Bicyclic α-Amino-ketones
Chemistry of Sodium Borohydride and Diborane. III. Synthesis of (+)-Lupinine by Hydroboration Reaction
Chemistry of Diborane and Sodium Borohydride. VIII. Imidate Formation from Nitriles with Sodium Borohydride
Ind. -N-Alkylation of Tryptophan and Synthesis of 1-Alkyltryptophan Hydrazides
Chemistry of Amino Acids. VII. The Synthesis and Spectral Studies of Some 2-Piperidones bearing β-Keto Ester Groups
Chemistry of Amino Acids. III. Reduction of Phenylalanine Ethyl Ester and Its Derivatives with Sodium Borohydride.
Stereochemical Studies. XII. Effects of Neighboring Functional Groups on 1,2-Asymmetric Induction in the Reduction of Propiophenone Derivatives by Catalytic Hydrogenation
A New Synthetic Method of 3,4-Dihydroisoquinoline Derivative by the Cyclodesulfurization of Thioamide
Studies on Thioamides. II. Application of Thioamides in Bischler-Napieralski Reaction.
Stereochemical Studies. XXXI. Total Synthesis of Several D-Pentose Derivatives. Stereochemical Courses of the Synthesis of Four Methyl 2,3-Anhydro-5-O-benzyl-D-pentofuranosides from L-Glutamic Acid and Their Reactions with Nucleophiles
Stereochemical Studies. XVI. Deaminative Acetolyses of L-Valine and L-Valine Benzyl Ester
Studies on Optically Active Amino Acids. XIX. Solvent Effects on Optical Rotatory Dispersion and Circular Dichroism of N-Dithiocarbethoxy-L-α-amino Acids
The Solvent Effects on the Optical Rotatory Dispersion of Dithiocarbamates of Amines
The Solvent Effects on the Optical Rotatory Dispersion of N-Thioacyl Derivatives of a-Amino Acids
The Solvent Effects on the Optical Rotatory Dispersion of Dithiocarbamates of α-Amino Acids
Amino Acids and Peptides. III. A New Synthetic Approach to N-Acylated α-Amino Aldehydes from N-Acylated α-Amino Acids by Catalytic Reduction of Their Mixed Carbonic-Carboxylic Acid Anhydrides with Palladium-Charcoal
Stereochemical Studies. XV. Neighboring Aryl Group Participation in Nitrous Acid Deaminations of L-Phenylalanine and Its p-Nitro and p-Methoxy Derivatives. Conversion of L-Phenylalanine to naturally Occurring S-Tropic Acid
Stereochemical Studies. XIV. Studies on the Neighboring Aryl Group Participation in Nitrous Acid Deaminations of L-Phenylalanine Ethyl Ester and Its p-Nitro and p-Methoxy Derivatives
Preparation and Nuclear Magnetic Resonance Spectra of Alkoxyamines
Stereochemical Studies. LII. Studies on the Stereochemical Courese in Deaminative Bromination of 3,5-Dichloro-L-tyrosine and in Amination of the Corresponding α-Bromo Acid. Existence of Strong Neighboring "Phenoxide"Group Participation
Amino Acids and peptides. XXVI. Phosphorus in Organic Synthesis. XV. Application of Diphenyl Phosphorazidate (DPPA) and Diethyl Phosphorocyanidate (DEPC) to the Synthesis of the N-Terminal Decapeptide of Gastric Inhibitory Polypeptide
Amino Acids and Peptides. XXV. Phosphorus in Organic Synthesis. XIV. Application of Diphenyl Phosphorazidate (DPPA) to the Synthesis of the N-Terminal Hexapeptide of the Vasoactive Intestinal Peptide
Chemistry of Sodium Borohydride and Diborane. IV. Reduction of Carboxylic Acids to Alcohols with Sodium Borohydride through Mixed Carbonic-Carboxylic Acid Anhydrides
Studies in the Indole Series. III. Steric Inhibition of Resonance in Cycloalkan [b] indolones.
Studies in the Indole Series. II. A General Synthesis of Cycloalkan[b]indolones
Stereochemical Studies. V. Intramolecular C-H Bond Insertion Reaction of Acyl Nitrene generated from optically Active Acyl Azide
Stereochemical Studies. IV. Studies on α-Alkyl-α-amino Acids. XII. Hofmann and Curtius Rearrangements of S (+)-2-Cyano-2-methyl-3-phenylpropionic Acid
Stereochemical Studies. III. Chemical Correlation of Absolute Configuration of 2-Cyano-2-methyl-3-phenylpropionic Acid to α-Methyl-α-isopropylsuccinic Acid
Studies on Thioamides. III. A New Synthetic Method of the 3,4-Dihydroisoquinoline Derivatives by the Cyclodesulfurization of Thioamides
Studies on Thioamides. IV. Extension of the Cyclodesulfurization Reaction to Synthesize 1-Substituted and 1,3-Disubstituted-3,4-dihydro-9H-pyrido [3,4-b] indole Derivatives
Studies on Optically Active Amino Acids. XVI. Studies on α-Alkyl-α-amino Acids. XI. Synthesis of R-α-Methylphenylalanine from S (+)-2-Methyl-3-phenylpropionic Acid by the Direct Conversion of the optically Active C-H Bond into the C-N Bond
Stereochemical Studies. II. Thermal and Photochemical Decompositions of Optically Active Alkyl Azidoformates
Stereochemical Studies. L. Reductive Decyanization of α-Amino Nitriles with Sodium in Liquid Ammonia. An Alternate Method for the Application to the Asymmetric Synthesis of optically Active Natural Products
Stereochemical Studies. XLIX. A Biogenetic-type Total Synthesis of Natural (+)-Maritidine from L-Tyrosine using highly Specific Asymmetric Cyclization
Stereochemical Studies. XVIII. Nitrous Acid Deaminations of threo- and erythro-Phenylserine and Their Methyl Esters in Acetic Acid
Stereochemical Studies. XI. Changes in the Stereochemical Course of 1,2-Asymmetric Induction in the Reduction of N-Substituted 2-Aminopropiophenone Derivatives with Sodium Borohydride
Stereochemical Studies. X. Effects of Neighboring Functional Groups on 1,2-Asymmetric Induction in the Reduction of Propiophenone Derivatives with Sodium Borohydride
Studies on Optically Active Amino Acids. III. Preparation of 3-(3,4-Dihydroxyphenyl)-DL-, -D-, and-L-alanine.
Studies on Optically Active Amino Acids. II. Partially Asymmetric Synthesis of 3-(3,4-Methylenedioxyphenyl) alanine.
Studies on Optically Active Amino Acids. I. Preparation of 3-(3,4-Methylenedioxyphenyl)-D-, and-L-alanine.

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